Hydrangea chinensis

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

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Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID64404e13af085054639115
Scientific name	Hydrangea chinensis
Authority	Maxim.
First published in	Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 , 10(16): 7 (1867)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Hydrangea subferruginca	W.W.Sm.	Notes Roy. Bot. Gard. Edinburgh 11: 212 (1919)
Hydrangea grossiserrata	Engl.	Nat. Pflanzenfam. (ed. 2) 18a: 207 1930
Hydrangea chloroleuca	Diels	Notizbl. Bot. Gart. Berlin-Dahlem 9: 1027 (1926)
Hydrangea subferruginea	W.W.Sm.	Notes Roy. Bot. Gard. Edinburgh 11: 212 (1919)
Hydrangea umbellata	Rehder	Pl. Wilson. 1: 25 (1911)
Hydrangea angustipetala	Hayata	J. Coll. Sci. Imp. Univ. Tokyo 30(1): 107 (1911)
Hydrangea obovatifolia	Hayata	Icon. Pl. Formosan. 3: 109 (1913)
Hydrangea angustifolia	Hayata	Icon. Pl. Formosan. 1: t. 32 1911
Hydrangea angustisepala	Hayata	Icon. Pl. Formosan. 2: 4 1912
Hydrangea angustipetala var. major	W.T.Wang & M.X.Nie	Bull. Bot. Res., Harbin 1(1-2): 51 (1981)
Hydrangea jiangxiensis	W.T.Wang & M.X.Nie	Bull. Bot. Res., Harbin 1(1-2): 52 (1981)
Hydrangea macrosepala	Hayata	Icon. Pl. Formosan. 3: 108 (1913)
Hydrangea glabrifolia	Hayata	Icon. Pl. Formosan. 3: 106 (1913)
Hydrangea formosana	Koidz.	Bot. Mag. (Tokyo) 43: 394 (1929)
Hydrangea scandens subsp. chinensis	(Maxim.) E.M.McClint.	J. Arnold Arbor. 37: 373 1956
Hydrangea pottingeri	Prain	J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 67: 290 (1899)
Hydrangea pubiramea	Merr.	Philipp. J. Sci., C 12: 267 (1917)
Hydrangea pubiramea var. parvifolia	Merr.	Philipp. J. Sci., C. 12: 268 1917
Hortensia chinensis	(Maxim.) H.Ohba & S.Akiyama	J. Jap. Bot. 91: 347 (2016)
Hydrangea scandens var. grosseserrata	(Engl.) Hatus.	Fl. Ryukyus : 305 (1971)

Common names Top

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Language	Common/alternative name
Arabic	هدرانج صيني
szy	nipaluma-balusin, balosin
Chinese	大风子
Chinese	甜茶
Chinese	土常山
Chinese	中国绣球
Chinese	中国绣球(. 伞形绣球）
Chinese	华八仙花根
Chinese	華八仙
Chinese	伞形绣球
Chinese	江西绣球
Chinese	狭瓣绣球
Chinese	绿瓣绣球

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Hydrangea chinensis var. lobbii	(Maxim.) Kitam.	Acta Phytotax. Geobot. 26: 6 (1974)
Hydrangea chinensis var. yaeyamensis	(Koidz.) T.Yamaz.	J. Jap. Bot. 75: 321 (2000)
Hydrangea chinensis var. yayeyamensis	(Koidz.) T.Yamaz.	J. Jap. Bot. 75(5): 321 (2000):.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China Southeast
- Eastern Asia
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indo-China
  - Myanmar
- Malesia
  - Philippines

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001135946
Tropicos	29101211
KEW	urn:lsid:ipni.org:names:791560-1
The Plant List	tro-29101211
Open Tree Of Life	486966
Observations.org	446660
NCBI Taxonomy	498914
IPNI	791560-1
GBIF	7319010
Freebase	/m/076vw4h
Elurikkus	587992
USDA GRIN	19448
Wikipedia	Hydrangea_chinensis
CMAUP	NPO22018

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Pest categorisation of Pyrrhoderma noxium

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

19-Mar-2024

PMCID:	PMC10949325
doi:	10.2903/j.efsa.2024.8667
PMID:	38505477

What Are the Effects of Moso Bamboo Expansion into Japanese Cedar on Arbuscular Mycorrhizal Fungi: Altering the Community Composition Rather than the Diversity

Zou G, Wu B, Chen B, Yang Y, Feng Y, Huang J, Liu Y, Murray PJ, Liu W

J Fungi (Basel)

18-Feb-2023

PMCID:	PMC9967659
doi:	10.3390/jof9020273
PMID:	36836387

Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health

Sun W, Shahrajabian MH

Molecules

15-Feb-2023

PMCID:	PMC9960276
doi:	10.3390/molecules28041845
PMID:	36838831

Neottia wuyishanensis (Orchidaceae: Neottieae), a new species from Fujian, China

Chen BH, Jin XH

Plant Divers

04-Feb-2021

PMCID:	PMC8591140
doi:	10.1016/j.pld.2021.01.008
PMID:	34816068

Anti-onchocerca Metabolites from Cyperus articulatus: Isolation, In Vitro Activity and In Silico ‘Drug-Likeness’

Metuge JA, Babiaka SB, Mbah JA, Ntie-Kang F, Ayimele GA, Cho-Ngwa F

Nat Prod Bioprospect

10-Jun-2014

PMCID:	PMC4111868
doi:	10.1007/s13659-014-0023-5
PMID:	25089243

A strong ‘filter’ effect of the East China Sea land bridge for East Asia’s temperate plant species: inferences from molecular phylogeography and ecological niche modelling of Platycrater arguta (Hydrangeaceae)

Qi XS, Yuan N, Comes HP, Sakaguchi S, Qiu YX

BMC Evol Biol

04-Mar-2014

PMCID:	PMC4015774
doi:	10.1186/1471-2148-14-41
PMID:	24593236

Secoiridoid glycoside and alkaloid constituents of Hydrangea chinensis.

Chang FR, Lee YH, Yang YL, Hsieh PW, Khalil AT, Chen CY, Wu YC

J Nat Prod

01-Sep-2003

doi:	10.1021/NP0302394
PMID:	14510608

Hydrachine A, a novel alkaloid from the roots of Hydrangea chinensis.

Patnam R, Chang FR, Chen CY, Kuo RY, Lee YH, Wu YC

J Nat Prod

01-Jul-2001

doi:	10.1021/NP010091T
PMID:	11473431

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1021/NP0302394
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1021/NP0302394
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
p-Anisaldehyde	31244	Click to see COC1=CC=C(C=C1)C=O	136.15	unknown	https://doi.org/10.1021/NP0302394
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde	8655	Click to see COC1=CC(=CC(=C1O)OC)C=O	182.17	unknown	https://doi.org/10.1021/NP010091T
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1021/NP0302394
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL	5366244	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1021/NP0302394
Phytol	5280435	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1021/NP0302394
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(1R,3S,3aS,5aR,5bS,6S,7aR,9S,11aS,13aS,13bS)-3a,5b,8,8,11a,13a-hexamethyl-3-propan-2-yl-1,2,3,4,5,5a,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysene-1,6,9-triol	162936373	Click to see CC(C)C1CC(C2C1(CCC3C2(CC=C4C3(C(CC5C4(CCC(C5(C)C)O)C)O)C)C)C)O	458.70	unknown	https://doi.org/10.1021/NP010091T
3a,5b,8,8,11a,13a-Hexamethyl-3-propan-2-yl-1,2,3,4,5,5a,6,7,7a,9,10,11,13,13b-tetradecahydrocyclopenta[a]chrysene-1,6,9-triol	162936372	Click to see CC(C)C1CC(C2C1(CCC3C2(CC=C4C3(C(CC5C4(CCC(C5(C)C)O)C)O)C)C)C)O	458.70	unknown	https://doi.org/10.1021/NP010091T
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Hydrangenoisde A	434883	Click to see COC(=O)C1=COC(C(C1CC2CC(=O)CC(O2)CC(=O)CCC3=CC=C(C=C3)O)C=C)OC4C(C(C(C(O4)CO)O)O)O	620.60	unknown	https://doi.org/10.1021/NP010091T
Hydrangenoside E	21589718	Click to see COC(=O)C1=COC(C(C1CC2CC(CC(O2)CCC3=CC=C(C=C3)O)O)C=C)OC4C(C(C(C(O4)CO)O)O)O	580.60	unknown	https://doi.org/10.1021/NP0302394
methyl (2S,3R,4R)-3-ethenyl-4-[[(2S,6S)-6-[4-(4-hydroxyphenyl)-2-oxobutyl]-4-oxooxan-2-yl]methyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	154496747	Click to see COC(=O)C1=COC(C(C1CC2CC(=O)CC(O2)CC(=O)CCC3=CC=C(C=C3)O)C=C)OC4C(C(C(C(O4)CO)O)O)O	620.60	unknown	https://doi.org/10.1021/NP010091T
methyl (2S,3R,4S)-3-ethenyl-4-[[(2S,6R)-6-(4-hydroxyphenyl)-4-oxooxan-2-yl]methyl]-2-[(2R,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	101759623	Click to see COC(=O)C1=COC(C(C1CC2CC(=O)CC(O2)C3=CC=C(C=C3)O)C=C)OC4C(C(C(C(O4)CO)O)O)O	550.60	unknown	https://doi.org/10.1021/NP0302394
methyl (2S,3R,4S)-3-ethenyl-4-[[(2S,6S)-6-[4-(4-hydroxyphenyl)-2-oxobutyl]-4-oxooxan-2-yl]methyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	21595218	Click to see COC(=O)C1=COC(C(C1CC2CC(=O)CC(O2)CC(=O)CCC3=CC=C(C=C3)O)C=C)OC4C(C(C(C(O4)CO)O)O)O	620.60	unknown	https://doi.org/10.1021/NP010091T
methyl (2S,3S,4R)-3-ethenyl-4-[[(2S,4S,6R)-4-hydroxy-6-[2-(4-hydroxyphenyl)ethyl]oxan-2-yl]methyl]-2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	154496749	Click to see COC(=O)C1=COC(C(C1CC2CC(CC(O2)CCC3=CC=C(C=C3)O)O)C=C)OC4C(C(C(C(O4)CO)O)O)O	580.60	unknown	https://doi.org/10.1021/NP0302394
methyl (2S,3S,4S)-3-ethenyl-4-[[(2S,6R)-6-(4-hydroxyphenyl)-4-oxooxan-2-yl]methyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	162896581	Click to see COC(=O)C1=COC(C(C1CC2CC(=O)CC(O2)C3=CC=C(C=C3)O)C=C)OC4C(C(C(C(O4)CO)O)O)O	550.60	unknown	https://doi.org/10.1021/NP0302394
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Diosgenin,dehydro	337494	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC=C6)C)C)C)OC1	396.60	unknown	via CMAUP database
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1021/NP0302394
Isoarborinol	12305182	Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1021/NP010091T
Isodiotigenin	46865737	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6O)O)O)C)C)C)OC1	448.60	unknown	via CMAUP database
Kogagenin	12304893	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6(C5(C(C(C(C6)O)O)O)C)O)C)C)OC1	464.60	unknown	via CMAUP database
Rubiarbonol B	12019474	Click to see CC(C)C1CC(C2C1(CCC3(C2(CC=C4C3C(CC5C4(CCC(C5(C)C)O)C)O)C)C)C)O	458.70	unknown	https://doi.org/10.1021/NP010091T
Sorghumol	621134	Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1021/NP010091T
Squalene	638072	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	https://doi.org/10.1021/NP0302394
Tokorogenin	20841762	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(C(C(C(C6)O)O)O)C)C)C)OC1	448.60	unknown	via CMAUP database
Yamogenin	441900	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
Yonogenin	12304416	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1	432.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
Dioscin	119245	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Disogluside	11827970	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1	576.80	unknown	via CMAUP database
Protoneogracillin	46906323	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1065.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	154496016	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1021/NP010091T
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	12314479	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/NP010091T
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/NP010091T
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/NP010091T
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1021/NP010091T
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1021/NP010091T
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid	1094	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	https://doi.org/10.1021/NP0302394
Shikimic acid	8742	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	https://doi.org/10.1021/NP0302394
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3S,4R,4aS)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	354447	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O	358.34	unknown	https://doi.org/10.1021/NP0302394
(3S,4S,4aS)-4-ethenyl-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	154497536	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O	358.34	unknown	https://doi.org/10.1021/NP0302394
7-epi-Vogeloside	102183193	Click to see COC1CC2C(C(OC=C2C(=O)O1)OC3C(C(C(C(O3)CO)O)O)O)C=C	388.40	unknown	https://doi.org/10.1021/NP0302394
Salidroside	159278	Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O	300.30	unknown	https://doi.org/10.1021/NP0302394
Sweroside	161036	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O	358.34	unknown	https://doi.org/10.1021/NP0302394
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	https://doi.org/10.1021/NP010091T https://doi.org/10.1021/NP0302394
p-Hydroxybenzaldehyde-d5	10701848	Click to see C1=CC(=CC=C1C=O)O	127.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(R)-3,4-Dihydro-8-hydroxy-3-(4-hydroxyphenyl)-1H-2-benzopyran-1-one	44144280	Click to see C1C(OC(=O)C2=C1C=CC=C2O)C3=CC=C(C=C3)O	256.25	unknown	https://doi.org/10.1021/NP010091T
Hydrangenol	119199	Click to see C1C(OC(=O)C2=C1C=CC=C2O)C3=CC=C(C=C3)O	256.25	unknown	https://doi.org/10.1021/NP010091T
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
1H-quinazolin-4-one	63112	Click to see C1=CC=C2C(=C1)C(=O)N=CN2	146.15	unknown	https://doi.org/10.1021/NP010091T
> Organoheterocyclic compounds / Quinolizines
3-(9-Hydroxy-2-oxo-1,3,4,6,7,8,9,9a-octahydroquinolizin-4-yl)quinazolin-4-one	73197336	Click to see C1CC(C2CC(=O)CC(N2C1)N3C=NC4=CC=CC=C4C3=O)O	313.35	unknown	https://doi.org/10.1021/NP010091T
3-[(3R,9S,9aR)-9-hydroxy-2-oxo-1,3,4,6,7,8,9,9a-octahydroquinolizin-3-yl]quinazolin-4-one	21589719	Click to see C1CC(C2CC(=O)C(CN2C1)N3C=NC4=CC=CC=C4C3=O)O	313.35	unknown	https://doi.org/10.1021/NP010091T
Hidrachine A	15519707	Click to see C1CC(C2CC(=O)CC(N2C1)N3C=NC4=CC=CC=C4C3=O)O	313.35	unknown	https://doi.org/10.1021/NP010091T
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-Propenoic acid, 3-(4-hydroxyphenyl)-, methyl ester	92203	Click to see COC(=O)C=CC1=CC=C(C=C1)O	178.18	unknown	https://doi.org/10.1021/NP010091T
Methyl 4-hydroxycinnamate	5319562	Click to see COC(=O)C=CC1=CC=C(C=C1)O	178.18	unknown	https://doi.org/10.1021/NP010091T
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1021/NP010091T
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Methoxycoumarin	10748	Click to see COC1=CC2=C(C=C1)C=CC(=O)O2	176.17	unknown	https://doi.org/10.1021/NP010091T
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
2H-1-Benzopyran-2-one, 5-hydroxy-	5318179	Click to see C1=CC(=C2C=CC(=O)OC2=C1)O	162.14	unknown	https://doi.org/10.1021/NP010091T
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
3,4,5,6,8-Pentadeuterio-7-hydroxychromen-2-one	45358955	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	167.17	unknown	via CMAUP database
7-Hydroxy-8-methoxycoumarin	5316302	Click to see COC1=C(C=CC2=C1OC(=O)C=C2)O	192.17	unknown	https://doi.org/10.1021/NP010091T
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1021/NP010091T

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Hydrangea chinensis

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